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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716458Generated: October 30, 2026

Hexane → 2-Bromo-5-methoxybenzyl bromide

https://huagongshe.com/reaction/716458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantBromineHCID 24408—
Reactant3-Methoxybenzyl bromideHCID 4067207—
SolventChloroformHCID 6212—
Product2-Bromo-5-methoxybenzyl bromideHCID 352595172.1%

Reaction Steps

To a solution of above-described crude 1-(bromomethyl)-3-methoxybenzene (152.5 g) in 1 L of chloroform a solution of 134 g (0.841 mol) of bromine in 200 ml of chloroform was added dropwise by vigorous stirring at room temperature. The reaction mixture was stirred overnight at ambient temperature and then evaporated to dryness. The residue was triturated with 1000 ml of n-hexane, and the precipitate was filtered off, washed with 100 ml of n-hexane, and then dried in vacuum. An additional amount of the product was obtained by evaporation of mother liquor followed by treatment of the residue with 200 ml of n-hexane. In total, this procedure gave 153 g (55% overall yield for two stages) of 1-bromo-2-(bromomethyl)-4-methoxybenzene. (average of two runs)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187583B2
Source datasetuspto-grants-2015_11
ORD IDord-06529ac9ae0a4d9cb5293fee4379941e
Source noteuspto-grants-2015_11